Literature DB >> 6404910

Synapsin I (protein I), a nerve terminal-specific phosphoprotein. I. Its general distribution in synapses of the central and peripheral nervous system demonstrated by immunofluorescence in frozen and plastic sections.

P De Camilli, R Cameron, P Greengard.   

Abstract

Synapsin I (formerly referred to as protein I) is the collective name for two almost identical phosphoproteins, synapsin Ia and synapsin Ib (protein Ia and protein Ib), present in the nervous system. Synapsin I has previously been shown by immunoperoxidase studies (De Camilli, P., T. Ueda, F. E. Bloom, E. Battenberg, and P. Greengard, 1979, Proc. Natl. Acad. Sci. USA, 76:5977-5981; Bloom, F. E., T. Ueda, E. Battenberg, and P. Greengard, 1979, Proc. Natl. Acad. Sci. USA 76:5982-5986) to be a neuron-specific protein, present in both the central and peripheral nervous systems and concentrated in the synaptic region of nerve cells. In those preliminary studies, the occurrence of synapsin I could be demonstrated in only a portion of synapses. We have now carried out a detailed examination of the distribution of synapsin I immunoreactivity in the central and peripheral nervous systems. In this study we have attempted to maximize the level of resolution of immunohistochemical light microscopy images in order to estimate the proportion of immunoreactive synapses and to establish their precise distribution. Optimal results were obtained by the use of immunofluorescence in semithin sections (approximately 1 micron) prepared from Epon-embedded nonosmicated tissues after the Epon had been removed. Our results confirm the previous observations on the specific localization of synapsin I in nerve cells and synapses. In addition, the results strongly suggest that, with a few possible exceptions involving highly specialized neurons, all synapses contain synapsin I. Finally, immunocytochemical experiments indicate that synapsin I appearance in the various regions of the developing nervous system correlates topographically and temporally with the appearance of synapses. In two accompanying papers (De Camilli, P., S. M. Harris, Jr., W. B. Huttner, and P. Greengard, and Huttner, W. B., W. Schiebler, P. Greengard, and P. De Camilli, 1983, J. Cell Biol. 96:1355-1373 and 1374-1388, respectively), evidence is presented that synapsin I is specifically associated with synaptic vesicles in nerve endings.

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Year:  1983        PMID: 6404910      PMCID: PMC2112636          DOI: 10.1083/jcb.96.5.1337

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  37 in total

1.  A manual of quantitative immunoelectrophoresis. Methods and applications. 1. General remarks on principles, equipment, reagents and procedures.

Authors:  B Weeke
Journal:  Scand J Immunol Suppl       Date:  1973

2.  Demonstration of central gamma-aminobutyrate-containing nerve terminals by means of antibodies against glutamate decarboxylase.

Authors:  M Pérez de la Mora; L D Possani; R Tapia; L Teran; R Palacios; K Fuxe; T Hökfelt; A Ljungdahl
Journal:  Neuroscience       Date:  1981       Impact factor: 3.590

3.  Distribution of protein I in mammalian brain as determined by a detergent-based radioimmunoassay.

Authors:  S E Goelz; E J Nestler; B Chehrazi; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1981-04       Impact factor: 11.205

4.  Two calcium/calmodulin-dependent protein kinases, which are highly concentrated in brain, phosphorylate protein I at distinct sites.

Authors:  M B Kennedy; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1981-02       Impact factor: 11.205

5.  Differential phosphorylation of multiple sites in purified protein I by cyclic AMP-dependent and calcium-dependent protein kinases.

Authors:  W B Huttner; L J DeGennaro; P Greengard
Journal:  J Biol Chem       Date:  1981-02-10       Impact factor: 5.157

6.  Dopamine and depolarizing agents regulate the state of phosphorylation of protein I in the mammalian superior cervical sympathetic ganglion.

Authors:  E J Nestler; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1980-12       Impact factor: 11.205

7.  Quantitative immunocytochemical localization of pancreatic secretory proteins in subcellular compartments of the rat acinar cell.

Authors:  M Bendayan; J Roth; A Perrelet; L Orci
Journal:  J Histochem Cytochem       Date:  1980-02       Impact factor: 2.479

8.  Widespread distribution of protein I in the central and peripheral nervous systems.

Authors:  P De Camilli; T Ueda; F E Bloom; E Battenberg; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1979-11       Impact factor: 11.205

9.  Immunocytochemical detection of peptides in osmicated and plastic-embedded tissue. An electron microscopic study.

Authors:  G Pelletier; R Puviani; O Bosler; L Descarries
Journal:  J Histochem Cytochem       Date:  1981-06       Impact factor: 2.479

10.  Serotonin stimulates phosphorylation of protein I in the facial motor nucleus of rat brain.

Authors:  A C Dolphin; P Greengard
Journal:  Nature       Date:  1981-01-01       Impact factor: 49.962

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  149 in total

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Authors:  Adriana Ferreira; Sabrina Paganoni
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2.  Biography of Pietro De Camilli.

Authors:  Liza Bundesen
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-24       Impact factor: 11.205

3.  Nerve agent exposure elicits site-specific changes in protein phosphorylation in mouse brain.

Authors:  Hongwen Zhu; Jennifer J O'Brien; James P O'Callaghan; Diane B Miller; Qiang Zhang; Minal Rana; Tiffany Tsui; Youyi Peng; John Tomesch; Joseph P Hendrick; Lawrence P Wennogle; Gretchen L Snyder
Journal:  Brain Res       Date:  2010-04-25       Impact factor: 3.252

4.  Differential expression of the p65 gene family.

Authors:  B Wendland; K G Miller; J Schilling; R H Scheller
Journal:  Neuron       Date:  1991-06       Impact factor: 17.173

5.  Airway epithelial cell expression of interleukin-6 in transgenic mice. Uncoupling of airway inflammation and bronchial hyperreactivity.

Authors:  B F DiCosmo; G P Geba; D Picarella; J A Elias; J A Rankin; B R Stripp; J A Whitsett; R A Flavell
Journal:  J Clin Invest       Date:  1994-11       Impact factor: 14.808

6.  Translocation of synapsin I in response to depolarization of isolated nerve terminals.

Authors:  T S Sihra; J K Wang; F S Gorelick; P Greengard
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

7.  Light- and electron-microscopic study of synaptic connections in the paracervical ganglion of the female rat: special reference to calcitonin gene-related peptide-, galanin- and tachykinin (substance P and neurokinin A)-immunoreactive nerve fibers and terminals.

Authors:  R E Papka; D L McNeill
Journal:  Cell Tissue Res       Date:  1993-03       Impact factor: 5.249

8.  Thrombospondin-4 and excitatory synaptogenesis promote spinal sensitization after painful mechanical joint injury.

Authors:  Nathan D Crosby; Frank Zaucke; Jeffrey V Kras; Ling Dong; Z David Luo; Beth A Winkelstein
Journal:  Exp Neurol       Date:  2014-12-05       Impact factor: 5.330

9.  Selective clustering of glutamate and gamma-aminobutyric acid receptors opposite terminals releasing the corresponding neurotransmitters.

Authors:  A M Craig; C D Blackstone; R L Huganir; G Banker
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-20       Impact factor: 11.205

10.  Nerve Terminal GABAA Receptors Activate Ca2+/Calmodulin-dependent Signaling to Inhibit Voltage-gated Ca2+ Influx and Glutamate Release.

Authors:  Philip Long; Audrey Mercer; Rahima Begum; Gary J Stephens; Talvinder S Sihra; Jasmina N Jovanovic
Journal:  J Biol Chem       Date:  2009-01-13       Impact factor: 5.157

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